Dynamic Polymer Free Volume Monitored by Single-Molecule Spectroscopy of a Dual Fluorescent Flapping Dopant

被引:27
作者
Goto, Yuma [1 ]
Omagari, Shun [1 ]
Sato, Ryuma [2 ]
Yamakado, Takuya [3 ]
Achiwa, Ryo [3 ]
Dey, Nilanjan [3 ,4 ]
Suga, Kensuke [3 ]
Vacha, Martin [1 ]
Saito, Shohei [3 ]
机构
[1] Tokyo Inst Technol, Dept Mat Sci & Engn, Sch Mat & Chem Engn, Meguro Ku, Tokyo 1528552, Japan
[2] Natl Inst Adv Ind Sci & Technol, Cellular & Mol Biotechnol Res Inst, Koto Ku, Tokyo 1350064, Japan
[3] Kyoto Univ, Grad Sch Sci, Sakyo Ku, Kyoto 6068502, Japan
[4] Birla Inst Technol & Sci Pilani, Dept Chem, Hyderabad 500078, Telangana, India
关键词
POSITRON-ANNIHILATION; PROBE; POLYSTYRENE; TEMPERATURE; DIFFUSION; HETEROGENEITY; ORIENTATION; VISCOSITY; FILMS;
D O I
10.1021/jacs.1c06428
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Single-molecule spectroscopy (SMS) of a dual fluorescent flapping molecular probe (N-FLAP) enabled real-time nanoscale monitoring of local free volume dynamics in polystyrenes. The SMS study was realized by structural improvement of a previously reported flapping molecule by nitrogen substitution, leading to increased brightness (22 times) of the probe. In a polystyrene thin film at the temperature of 5 K above the glass transition, the spectra of a single N-FLAP molecule undergo frequent jumps between short- and long-wavelength forms, the latter one indicating planarization of the molecule in the excited state. The observed spectral jumps were statistically analyzed to reveal the dynamics of the molecular environment. The analysis together with MD and QM/MM calculations show that the excited-state planarization of the flapping probe occurs only when sufficiently large polymer free volume of more than, at least, 280 angstrom(3) is available close to the molecule, and that such free volume lasts for an average of 1.2 s.
引用
收藏
页码:14306 / 14313
页数:8
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